X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
ganglioside (2) 2
analysis (1) 1
animals (1) 1
beta-hexosaminidase activity (1) 1
bioactive peptid (1) 1
biochemistry & molecular biology (1) 1
biology (1) 1
brain (1) 1
brain chemistry - genetics (1) 1
catabolism (1) 1
cathepsin a (1) 1
cathepsins (1) 1
chemical properties (1) 1
cytoplasmic vesicles - pathology (1) 1
gangliosidoses, gm2 - genetics (1) 1
gangliosidoses, gm2 - metabolism (1) 1
gliosis - genetics (1) 1
gliosis - pathology (1) 1
glycosphingolipids - metabolism (1) 1
gm2 (1) 1
hexa gene (1) 1
hexosaminidase (1) 1
hexosaminidase b - genetics (1) 1
index medicus (1) 1
lameness, animal - genetics (1) 1
lysosomal storage (1) 1
lysosome (1) 1
lysosomes (1) 1
male (1) 1
medicine (1) 1
mice (1) 1
mice, inbred c57bl (1) 1
mice, knockout (1) 1
molecular biosciences (1) 1
mouse (1) 1
mouse model (1) 1
neuraminidase (1) 1
neuraminidase - deficiency (1) 1
neuraminidase - genetics (1) 1
neurons - pathology (1) 1
neurosciences (1) 1
original research (1) 1
peptides (1) 1
physiological aspects (1) 1
plasma-membrane (1) 1
purkinje cells - pathology (1) 1
regulation (1) 1
research (1) 1
research paper (1) 1
sialidase neu3 (1) 1
site-directed mutagenesis (1) 1
spectrometry, mass, matrix-assisted laser desorption-ionization (1) 1
targeted disruption (1) 1
tay-sachs (1) 1
tay-sachs disease (1) 1
tay-sachs disease - genetics (1) 1
tay-sachs disease - pathology (1) 1
tay–sachs (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Frontiers in Molecular Biosciences, ISSN 2296-889X, 10/2016, Volume 3, p. 68
Lysosomal serine carboxypeptidase Cathepsin A (CTSA) is a multifunctional enzyme with distinct protective and catalytic function. CTSA present in the lysosomal... 
Cathepsin A | Regulation | Mouse | Lysosome | Bioactive peptid | mouse | bioactive peptid | regulation | lysosome | BIOCHEMISTRY & MOLECULAR BIOLOGY | Peptides | Analysis | Cathepsins | Lysosomes | Physiological aspects | Chemical properties | Research
Journal Article
Molecular Genetics and Metabolism Reports, ISSN 2214-4269, 09/2015, Volume 4, Issue C, pp. 72 - 82
Tay–Sachs disease is a severe lysosomal storage disorder caused by mutations in the HEXA gene coding for α subunit of lysosomal β-Hexosaminidase A enzyme,... 
Ganglioside | Tay–Sachs | Neuraminidase | Hexosaminidase
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.